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Structure of 61494-55-1
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This acetic acid derivative features a chloropyridinyl moiety that enhances electronic modulation and metabolic stability. It integrates readily into bioactive scaffolds, serving as a key building block in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
2-(2-Chloropyridin-3-yl)acetic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-containing bioactive scaffolds. Its chloro-substituted pyridine ring facilitates downstream functionalization via palladium-catalyzed cross-coupling, while the carboxylic acid group supports direct derivatization or amide formation. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis campaigns in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: